Hot Spot and Itch Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Hot Spot and Itch Relief

FidoPharmBrands, LLC
FidoPharmBrands, LLC

VETTRUST MEDICATED HOT SPOT AND ITCH RELIEF SPRAY




FULL PRESCRIBING INFORMATION

FRONT PANEL






















From the makers of PetArmor, VetTrust Hot Spot and Itch Relief Spray is specially formulated
with hydrocortisone and pramoxine to reduce pain, itching, and inflammation associated
with hot spots. By reducing the itching and irritation, this spray can also help reduce
excessive licking and chewing to allow healing to begin.

Active ingredient

ACTIVE INGREDIENTS: 0.5% HYDROCORTISONE, 0.25% PRAMOXINE HCI.

INACTIVE INGREDIENTS: PURIFIED WATER, ACRYLATES COPOLYMER, GLYCERINE, PEG-7
DIMETHICONE, AVENA SATIVA (OATMEAL) EXTRACT, ALOE BARBADENSIS (ALOE VERA) LEAF JUICE,
FRAGRANCE, METHYLISOTHIAZOLINONE, TRIETHANOLAMINE.

Directions for Use: SHAKE WELL. For dry application - apply directly to skin and haircoat and allow to
dry. For wet application or after shampooing - remove excess moisture and apply directly to skin and
haircoat. Use as often as needed or as directed by veterinarian.

Caution: For topical use only. Avoid contact with eyes. If skin
irritation develops or increases or you see no improvement,
stop use and call your veterinarian. Keep out of the reach of
children and pets. Wash hands after use.

Store at controlled room temperature of 15 - 30° C (59 - 86° F).

Questions? Comments? 1-855-908-PETS (7387)
www.petarmor.com/vettrust
Distributed by FidoPharm
PO Box 1060, Yardley, PA 19067-9060
©2012 FidoPharmBrands, LLC.
All rights reserved.

NDC # 433-036-01





Spray Bottle Label

Hot Spot and Itch Relief

Hot Spot and Itch Relief

Hydrocortisone, Pramoxine SPRAY

Product Information

Product Type Otc animal drug label Item Code (Source) NDC:43369-036
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Hydrocortisone HYDROCORTISONE 0.59 mg
pramoxine hydrochloride PRAMOXINE 0.295 mg

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43369-036-01 118 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-03-04


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Be sure to consult your doctor before taking any medication!
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